Abstract
ObjectivesThe goal of this study was to evaluate the long-term impact of repeated (r) mild traumatic brain injury (mTBI) on the healing of fractures in a mouse model. Ten week-old male mice were subjected to r-mTBI once per day for 4 days followed by closed femoral fracture using a three-point bending technique, 1 week post impact and fracture healing phenotype evaluated at 20 weeks of age.ResultsMicro-CT analysis of the fracture callus region at nine weeks post fracture revealed reduced bone volume (30%, p < 0.05) in the r-mTBI fracture group compared to the control-fracture group. The connectivity density of the fracture callus bone was reduced by 40% (p < 0.01) in the r-mTBI fracture group. Finite element analysis of the fracture callus region showed reduced failure load (p = 0.08) in the r-mTBI group compared to control group. There was no residual cartilage in the fracture callus region of either the r-mTBI or control fracture group. The reduced fracture callus bone volume and mechanical strength of fracture callus in r-mTBI mice 9 weeks post fracture are consistent with negative effects of r-mTBI on fracture healing over a long-term resulting in decreased mechanical strength of the fracture callus.
Highlights
Traumatic brain injury (TBI) is an acute injury that occurs as a result of an external force caused by falls, accidents, sports injuries and military conflicts [1, 2] and can be classified into three forms: mild, moderate, and severe
By using a mouse model of mild traumatic brain injury (mTBI), we have demonstrated that Repeated mild traumatic brain injury (r-mTBI) decreased trabecular bone formation and that this reduction was in part due to a deficiency in the growth hormone (GH)-Insulin-like growth factor-1 (IGF-I) axis [13]
Because r-mTBI has a negative effect on bone formation via a mechanism that involved the GH/insulin-like growth factor (IGF)-I axis [13], we determined the impact of r-mTBI on healing of fractured bone in a mouse model
Summary
Micro-CT analysis of the fracture callus region at nine weeks post fracture revealed reduced bone volume (30%, p < 0.05) in the r-mTBI fracture group compared to the control-fracture group. The connectivity density of the fracture callus bone was reduced by 40% (p < 0.01) in the r-mTBI fracture group. Finite element analysis of the fracture callus region showed reduced failure load (p = 0.08) in the r-mTBI group compared to control group. There was no residual cartilage in the fracture callus region of either the r-mTBI or control fracture group. The reduced fracture callus bone volume and mechanical strength of fracture callus in r-mTBI mice 9 weeks post fracture are consistent with negative effects of r-mTBI on fracture healing over a long-term resulting in decreased mechanical strength of the fracture callus
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